TW200911822A - Boron-containing small molecules - Google Patents
Boron-containing small molecules Download PDFInfo
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- TW200911822A TW200911822A TW097123257A TW97123257A TW200911822A TW 200911822 A TW200911822 A TW 200911822A TW 097123257 A TW097123257 A TW 097123257A TW 97123257 A TW97123257 A TW 97123257A TW 200911822 A TW200911822 A TW 200911822A
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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Landscapes
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- General Health & Medical Sciences (AREA)
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EP (1) | EP2164331B1 (de) |
JP (3) | JP5530923B2 (de) |
KR (3) | KR20150100945A (de) |
CN (2) | CN101772302B (de) |
AR (1) | AR067105A1 (de) |
AU (1) | AU2008265630B2 (de) |
BR (1) | BRPI0813450B8 (de) |
CA (1) | CA2692135C (de) |
CL (1) | CL2008001855A1 (de) |
CO (1) | CO6251209A2 (de) |
CR (1) | CR11224A (de) |
DK (1) | DK2164331T3 (de) |
DO (1) | DOP2009000281A (de) |
EA (1) | EA020530B1 (de) |
ES (1) | ES2655299T3 (de) |
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PE (1) | PE20090840A1 (de) |
SG (1) | SG182219A1 (de) |
TW (1) | TW200911822A (de) |
UY (1) | UY31171A1 (de) |
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Families Citing this family (67)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2987796B1 (de) | 2005-02-16 | 2018-08-08 | Anacor Pharmaceuticals, Inc. | Halogen-substituierte boronophthalide zur behandlung von infektionen |
US7767657B2 (en) * | 2005-02-16 | 2010-08-03 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
CN101420854B (zh) | 2006-02-16 | 2013-08-07 | 安纳考尔医药公司 | 作为抗炎药的含硼的小分子 |
EP2015757A4 (de) | 2006-05-02 | 2011-01-26 | Anacor Pharmaceuticals Inc | Hydrolyseresistente, borhaltige therapeutika verwendungsverfahren |
JO3396B1 (ar) * | 2007-06-20 | 2019-10-20 | Anacor Pharmaceuticals Inc | جزيئات صغيرة تحتوي على البورون |
KR101672511B1 (ko) | 2008-03-06 | 2016-11-03 | 아나코르 파마슈티칼스 인코포레이티드 | 소염제로써 붕소가 함유된 소분자 |
WO2009140309A2 (en) * | 2008-05-12 | 2009-11-19 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
WO2010028005A1 (en) | 2008-09-04 | 2010-03-11 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
WO2010027975A1 (en) | 2008-09-04 | 2010-03-11 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
US9493489B2 (en) | 2008-10-15 | 2016-11-15 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules as anti-protozoal agents |
JP2012512262A (ja) * | 2008-12-17 | 2012-05-31 | アナコール ファーマシューティカルズ,インコーポレーテッド | (s)−3−アミノメチル−7−(3−ヒドロキシ−プロポキシ)−3h−ベンゾ[c][1,2]オキサボロール−1−オールの多形体 |
WO2010132833A1 (en) * | 2009-05-14 | 2010-11-18 | The Regents Of The University Of Michigan | Streptococcus vaccine compositions and methods of using the same |
BR112012001987A2 (pt) | 2009-07-28 | 2015-09-01 | Anacor Pharmaceuticals Inc | Composto, combinação, formulação farmacêutica, uso de um composto, uma combinação ou um sal farmaceuticamente aceitável dos mesmos, e, métodos para tratar uma infecção bacteriana, para matar ou inibir o crescimento de uma bactéria, e para inibir uma beta-lactamase. |
WO2011019616A1 (en) | 2009-08-14 | 2011-02-17 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules as antiprotozoal agents |
WO2011019612A1 (en) | 2009-08-14 | 2011-02-17 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules as antiprotozoal agents |
US9440994B2 (en) | 2009-08-14 | 2016-09-13 | Anacor Pharmaceuticals, Inc. | Boron containing small molecules as antiprotozoal agents |
US20110207701A1 (en) * | 2009-08-19 | 2011-08-25 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules as antiprotozoal agents |
US20110124597A1 (en) * | 2009-09-25 | 2011-05-26 | Anacor Pharmaceuticals, Inc. | Boron containing small molecules |
US8979820B2 (en) | 2009-10-09 | 2015-03-17 | Cynthia S. Bailey | Method and apparatus for improving the appearance of nails affected by onychomycosis through the topical application of an aqueous solution containing boric acid and camphor or other terpenes |
WO2011049971A1 (en) | 2009-10-20 | 2011-04-28 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules as antiprotozoal agents |
WO2011060196A1 (en) * | 2009-11-11 | 2011-05-19 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
WO2011094450A1 (en) | 2010-01-27 | 2011-08-04 | Anacor Pharmaceuticals, Inc | Boron-containing small molecules |
WO2011116348A1 (en) | 2010-03-19 | 2011-09-22 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules as anti-protozoal agent |
TWI503324B (zh) * | 2010-04-07 | 2015-10-11 | Glaxosmithkline Llc | 苯并氧雜硼之製備方法 |
DK2613788T3 (en) * | 2010-09-07 | 2017-08-07 | Anacor Pharmaceuticals Inc | BENZOXABOROLD DERIVATIVES FOR TREATMENT OF BACTERIA INFECTIONS |
WO2013025975A1 (en) * | 2011-08-17 | 2013-02-21 | Glaxosmithkline Llc | Combination treatments for hepatitis c |
WO2013049424A1 (en) | 2011-09-28 | 2013-04-04 | Wisconsin Alumni Research Foundation | Catalytic conversion of cellulose to fuels and chemicals using boronic acids |
AR088668A1 (es) | 2011-11-21 | 2014-06-25 | Lilly Co Eli | Moleculas pequeñas que contienen boro |
AR088669A1 (es) | 2011-11-21 | 2014-06-25 | Lilly Co Eli | Derivados de dihidrodibenzo[c][1,2]oxaborol y dihidroisoxazol utiles para el control de ectoparasitos |
CN104136032B (zh) * | 2011-12-22 | 2018-11-13 | 盟科医药技术公司 | 可用于抗菌治疗的三环类硼化合物 |
US20150080342A1 (en) * | 2012-04-14 | 2015-03-19 | Anacor Pharmaceuticals, Inc. | Benzoxaborole compounds and uses thereof |
US9585396B2 (en) | 2013-01-30 | 2017-03-07 | Agrofresh Inc. | Volatile applications against pathogens |
US10070649B2 (en) | 2013-01-30 | 2018-09-11 | Agrofresh Inc. | Volatile applications against pathogens |
US8669207B1 (en) | 2013-01-30 | 2014-03-11 | Dow Agrosciences, Llc. | Compounds and compositions |
US11039617B2 (en) | 2013-01-30 | 2021-06-22 | Agrofresh Inc. | Large scale methods of uniformly coating packaging surfaces with a volatile antimicrobial to preserve food freshness |
PE20151299A1 (es) | 2013-01-30 | 2015-09-18 | Dow Agrosciences Llc | Uso de benzoxaboroles como agentes antimicrobianos volatiles en carnes, plantas o partes de plantas |
US9452173B2 (en) | 2013-01-31 | 2016-09-27 | Merz Pharmaceuticals, Llc | Topical compositions and methods for making and using same |
US9433680B2 (en) | 2013-01-31 | 2016-09-06 | Merz Pharmaceuticals, Llc | Topical compositions and methods for making and using same |
US8778365B1 (en) | 2013-01-31 | 2014-07-15 | Merz Pharmaceuticals, Llc | Topical compositions and methods for making and using same |
US9446131B2 (en) | 2013-01-31 | 2016-09-20 | Merz Pharmaceuticals, Llc | Topical compositions and methods for making and using same |
AP2015008638A0 (en) | 2013-02-01 | 2015-08-31 | Anacor Pharmaceuticals Inc | Boron-containing small molecules as antiprotozoal agents |
AU2014202928B1 (en) * | 2013-06-05 | 2014-09-11 | Agrofresh Inc. | Compounds and compositions |
KR101636431B1 (ko) * | 2013-07-30 | 2016-07-05 | 동아에스티 주식회사 | 트리사이클릭 벤즈옥사보롤 화합물, 이의 제조방법 및 용도 |
HRP20220384T1 (hr) * | 2013-08-09 | 2022-07-22 | Glaxosmithkline Intellectual Property (No. 2) Limited | Triciklički benzoksaborol spojevi i njihove uporabe |
EA038093B1 (ru) * | 2013-12-20 | 2021-07-05 | Глаксосмитклайн Интеллекчуал Проперти (№2) Лимитед | Способ лечения заболевания, вызванного инфекцией комплекса mycobacterium tuberculosis, с использованием (s)-(3-хлор-7,8-дигидро-2h-1,6,9-триокса-9a-борабензо[cd]азулен-2-ил)метанамина или его фармацевтически приемлемой соли |
WO2015121442A1 (en) * | 2014-02-17 | 2015-08-20 | Syngenta Participations Ag | Microbiocidally active benzoxaboroles |
KR20170024068A (ko) | 2014-07-01 | 2017-03-06 | 다이이찌 산쿄 가부시키가이샤 | 항박테리아제로서의 삼환식 벤즈옥사보롤 |
EP3212196A4 (de) * | 2014-10-29 | 2018-07-11 | Wisconsin Alumni Research Foundation | Boronsäurehemmer der hiv-protease |
MA41494B1 (fr) | 2015-02-12 | 2020-10-28 | Glaxosmithkline Ip No 2 Ltd | Composés benzoxaborole substitués en position 4 et utilisations associées |
WO2016164589A1 (en) | 2015-04-09 | 2016-10-13 | The Penn State Research Foundation | Synergistic benzoxaborole-containing anti-fungicidal composition |
US10160867B2 (en) * | 2015-08-06 | 2018-12-25 | The Penn State Research Foundation | Benzoxaborole-containing coating resistant to cellulose-supportable fungus |
US10874679B2 (en) | 2016-03-02 | 2020-12-29 | Bill & Melinda Gates Foundation | Boron-containing small molecules |
CN109152932B (zh) | 2016-03-02 | 2021-09-28 | 比尔及梅琳达盖茨基金会 | 含硼小分子 |
EP3423065B1 (de) | 2016-03-02 | 2021-07-21 | Anacor Pharmaceuticals, Inc. | Borhaltige kleine moleküle |
TW201735792A (zh) | 2016-03-07 | 2017-10-16 | 農業保鮮股份有限公司 | 使用苯并氧雜硼雜環戊烯化合物和防腐氣體作為作物的抗微生物劑之協同方法 |
KR102231489B1 (ko) | 2016-05-12 | 2021-03-23 | 아나코르 파마슈티칼스 인코포레이티드 | 기생충 질병을 치료하기 위한 신규 화합물 |
MA52337A (fr) | 2017-03-01 | 2021-03-03 | Anacor Pharmaceuticals Inc | Nouveaux analogues d'oxaborole et utilisations de ces derniers |
CN107090000B (zh) * | 2017-04-27 | 2019-07-12 | 上海交通大学 | 一种苯并硼唑7位脂肪酸的衍生物及其制备与用途 |
US11944435B2 (en) | 2017-06-13 | 2024-04-02 | Vdi Laboratory, Llc | System and procedure for stabilizing, storing and recovering blood samples |
WO2019108982A1 (en) * | 2017-11-30 | 2019-06-06 | Boragen, Inc. | Benzoxaborole compounds and formulations thereof |
US20190159457A1 (en) * | 2017-11-30 | 2019-05-30 | Boragen, Inc. | Combinatorial Compositions of Benzoxaboroles and Biologic Agents |
EP3836938A4 (de) | 2018-08-18 | 2022-05-11 | Boragen, Inc. | Feste formen von substituiertem benzoxazol und zusammensetzungen davon |
AR116305A1 (es) * | 2018-09-07 | 2021-04-21 | Boragen Inc | Compuestos que contienen boro y sus usos |
US11058695B2 (en) * | 2019-11-08 | 2021-07-13 | Myongji University Industry And Academia Cooperation Foundation | Inhibitor of carbapenem-hydrolyzing class D beta-lactamases |
EP4204012A1 (de) | 2020-08-31 | 2023-07-05 | Pfizer Inc. | Verfahren zum schutz von rna |
EP4384527A1 (de) * | 2022-06-23 | 2024-06-19 | Micurx Pharmaceuticals, Inc. | Prodrugs von borverbindungen und ihre verwendung bei der behandlung von bakteriellen infektionen |
AU2023287202A1 (en) * | 2022-06-23 | 2024-06-06 | Shanghai Micurx Pharmaceutical Co., Ltd. | Methods and uses of boron compounds in the treatment of nontuberculous mycobacterium infections and pharmaceutical compositions for treatment of same |
Family Cites Families (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2260336A (en) | 1939-10-16 | 1941-10-28 | Dow Chemical Co | Method of preparation of organic borates |
GB1396904A (en) * | 1972-08-11 | 1975-06-11 | Ici Ltd | Method for the control of micro-organisms |
US5962498A (en) | 1986-06-11 | 1999-10-05 | Procyon Pharmaceuticals, Inc. | Protein kinase C modulators. C. indolactam structural-types with anti-inflammatory activity |
US4919934A (en) | 1989-03-02 | 1990-04-24 | Richardson-Vicks Inc. | Cosmetic sticks |
US5594151A (en) | 1994-01-28 | 1997-01-14 | Prolinx, Inc. | Phenylboronic acid complexing reagents derived from aminosalicylic acid |
GB9411587D0 (en) * | 1994-06-09 | 1994-08-03 | Zeneca Ltd | Compound, composition and use |
US6083903A (en) | 1994-10-28 | 2000-07-04 | Leukosite, Inc. | Boronic ester and acid compounds, synthesis and uses |
US5831046A (en) | 1996-08-05 | 1998-11-03 | Prolinx, Incorporated | Boronic acid-contaning nucleic acid monomers |
US6306628B1 (en) | 1999-08-25 | 2001-10-23 | Ambergen, Incorporated | Methods for the detection, analysis and isolation of Nascent proteins |
US6369098B1 (en) | 1999-10-05 | 2002-04-09 | Bethesda Pharmaceuticals, Inc. | Dithiolane derivatives |
CA2415938A1 (en) | 2000-07-14 | 2002-01-24 | Zycos Inc. | Alpha-msh related compounds and methods of use |
US6537733B2 (en) * | 2001-02-23 | 2003-03-25 | Applied Materials, Inc. | Method of depositing low dielectric constant silicon carbide layers |
GB0117645D0 (en) | 2001-07-19 | 2001-09-12 | Isis Innovation | Therapeutic stratergies for prevention and treatment of alzheimers disease |
DE10143979A1 (de) | 2001-09-07 | 2003-03-27 | Clariant Gmbh | Verfahren zur Herstellung von Bisallylboranen und nicht-aromatischen Boronsäuren |
EP1444981A1 (de) | 2001-10-11 | 2004-08-11 | Katsuhiko Mikoshiba | Mittel zur unterdrückung der zunahme der intrazellulären calciumkonzentration |
CN1325504C (zh) | 2002-01-10 | 2007-07-11 | 宾夕法尼亚州研究基金会 | 制备二芳基硼酸烷基酯和络合的二芳基硼酸的方法 |
CA2484822A1 (en) * | 2002-05-28 | 2003-12-04 | 3-Dimensional Pharmaceuticals, Inc. | Novel thiophene amidines, compositions thereof, and methods of treating complement-mediated diseases and conditions |
US7465836B2 (en) * | 2003-06-16 | 2008-12-16 | Anacor Pharmaceuticals, Inc. | Hydrolytically-resistant boron-containing therapeutics and methods of use |
EP2335722B1 (de) | 2004-05-12 | 2019-03-13 | The Brigham and Women's Hospital, Inc. | Verwendung von Gelsolin zur Behandlung von Infektionen |
US7767657B2 (en) | 2005-02-16 | 2010-08-03 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
EP2987796B1 (de) * | 2005-02-16 | 2018-08-08 | Anacor Pharmaceuticals, Inc. | Halogen-substituierte boronophthalide zur behandlung von infektionen |
CN101420854B (zh) * | 2006-02-16 | 2013-08-07 | 安纳考尔医药公司 | 作为抗炎药的含硼的小分子 |
MX2008015918A (es) | 2006-06-12 | 2009-01-14 | Anacor Pharmaceuticals Inc | Compuestos para el tratamiento de enfermedad periodontal. |
US20070286822A1 (en) | 2006-06-12 | 2007-12-13 | Anacor Pharmaceuticals Inc. | Compounds for the Treatment of Periodontal Disease |
DE102006038471A1 (de) | 2006-08-17 | 2008-04-10 | Wala-Heilmittel Gmbh | Platanencreme, Verfahren zu ihrer Herstellung und Verwendung |
JO3396B1 (ar) * | 2007-06-20 | 2019-10-20 | Anacor Pharmaceuticals Inc | جزيئات صغيرة تحتوي على البورون |
WO2009140309A2 (en) * | 2008-05-12 | 2009-11-19 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
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